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Shenzhen Jiefu Industry Development Co

⚠️ Moderate Risk

FEI: 3007523142 • Shenzhen • CHINA

FEI

FEI Number

3007523142

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Ltddongmen South Road No. 6, , Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

34.0
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
2
Unique Violations
4/29/2010
Latest Refusal
5/19/2009
Earliest Refusal

Score Breakdown

Violation Severity
66.7×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

752×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
4/29/2010
66BAY44NICOTINE DELIVERY SYSTEM
75UNAPPROVED
New Orleans District Office (NOL-DO)
5/19/2009
66BAQ44NICOTINE DELIVERY SYSTEM
333LACKS FIRM
75UNAPPROVED
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Shenzhen Jiefu Industry Development Co's FDA import refusal history?

Shenzhen Jiefu Industry Development Co (FEI: 3007523142) has 2 FDA import refusal record(s) in our database, spanning from 5/19/2009 to 4/29/2010.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Shenzhen Jiefu Industry Development Co's FEI number is 3007523142.

What types of violations has Shenzhen Jiefu Industry Development Co received?

Shenzhen Jiefu Industry Development Co has been cited for 2 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about Shenzhen Jiefu Industry Development Co come from?

All FDA import refusal data for Shenzhen Jiefu Industry Development Co is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.